Intestinal homeostasis disruption in mice chronically exposed to arsenite-contaminated drinking water

Chronic exposure to inorganic arsenic [As(III) and As(V)] affects about 200 million people, and is linked to a greater incidence of certain types of cancer. Drinking water is the main route of exposure, so, in endemic areas, the intestinal mucosa is constantly exposed to the metalloid. However, studies on the intestinal toxicity of inorganic As are scarce. The objective of this study was to evaluate the toxicity of a chronic exposure to As(III) on the intestinal mucosa and its associated microbiota. For this purpose, BALB/c mice were exposed during 6 months through drinking water to As(III) (15 and 30 mg/L). Treatment with As(III) increased reactive oxygen species (43-64%) and lipid peroxidation (8-51%). A pro-inflammatory response was also observed, evidenced by an increase in fecal lactoferrin (23-29%) and mucosal neutrophil infiltration. As(III) also induced an increase in the colonic levels of pro-inflammatory cytokines (24-201%) and the activation of some pro-inflammatory signaling pathways. Reductions in the number of goblet cells and mucus production were also observed. Moreover, As(III) exposure resulted in changes in gut microbial alpha diversity but no differences in beta diversity. This suggested that the abundance of some taxa was significantly affected by As(III), although the composition of the population did not show significant alterations. Analysis of differential taxa agreed with this, 21 ASVs were affected in abundance or variability, especially ASVs from the family Muribaculaceae. Intestinal microbiota metabolism was also affected, as reductions in fecal concentration of short-chain fatty acids were observed. The effects observed on different components of the intestinal barrier may be responsible of the increased permeability in As(III) treated mice, evidenced by an increase in fecal albumin (48-66%). Moreover, serum levels of Lipopolysaccharide binding proteins and TNF-α were increased in animals treated with 30 mg/L of As(III), suggesting a low-level systemic inflammation.

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Main Authors: Domene, Adrián, Orozco, Helena, Rodríguez Viso, Pilar, Monedero, Vicente, Zúñiga, Manuel, Vélez, Dinoraz, Devesa, Vicenta
Other Authors: Agencia Estatal de Investigación (España)
Format: artículo biblioteca
Language:English
Published: Elsevier 2023-02-16
Subjects:Barrier impairment, Inflammation, Inorganic arsenic, Intestinal microbiota, Intestinal mucosa, Metabolic endotoxemia, http://metadata.un.org/sdg/3, Ensure healthy lives and promote well-being for all at all ages,
Online Access:http://hdl.handle.net/10261/296901
http://dx.doi.org/10.13039/501100000780
http://dx.doi.org/10.13039/501100011033
https://api.elsevier.com/content/abstract/scopus_id/85148963688
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spelling dig-iata-es-10261-2969012024-05-14T20:39:05Z Intestinal homeostasis disruption in mice chronically exposed to arsenite-contaminated drinking water Domene, Adrián Orozco, Helena Rodríguez Viso, Pilar Monedero, Vicente Zúñiga, Manuel Vélez, Dinoraz Devesa, Vicenta Agencia Estatal de Investigación (España) European Commission Barrier impairment Inflammation Inorganic arsenic Intestinal microbiota Intestinal mucosa Metabolic endotoxemia http://metadata.un.org/sdg/3 Ensure healthy lives and promote well-being for all at all ages Chronic exposure to inorganic arsenic [As(III) and As(V)] affects about 200 million people, and is linked to a greater incidence of certain types of cancer. Drinking water is the main route of exposure, so, in endemic areas, the intestinal mucosa is constantly exposed to the metalloid. However, studies on the intestinal toxicity of inorganic As are scarce. The objective of this study was to evaluate the toxicity of a chronic exposure to As(III) on the intestinal mucosa and its associated microbiota. For this purpose, BALB/c mice were exposed during 6 months through drinking water to As(III) (15 and 30 mg/L). Treatment with As(III) increased reactive oxygen species (43-64%) and lipid peroxidation (8-51%). A pro-inflammatory response was also observed, evidenced by an increase in fecal lactoferrin (23-29%) and mucosal neutrophil infiltration. As(III) also induced an increase in the colonic levels of pro-inflammatory cytokines (24-201%) and the activation of some pro-inflammatory signaling pathways. Reductions in the number of goblet cells and mucus production were also observed. Moreover, As(III) exposure resulted in changes in gut microbial alpha diversity but no differences in beta diversity. This suggested that the abundance of some taxa was significantly affected by As(III), although the composition of the population did not show significant alterations. Analysis of differential taxa agreed with this, 21 ASVs were affected in abundance or variability, especially ASVs from the family Muribaculaceae. Intestinal microbiota metabolism was also affected, as reductions in fecal concentration of short-chain fatty acids were observed. The effects observed on different components of the intestinal barrier may be responsible of the increased permeability in As(III) treated mice, evidenced by an increase in fecal albumin (48-66%). Moreover, serum levels of Lipopolysaccharide binding proteins and TNF-α were increased in animals treated with 30 mg/L of As(III), suggesting a low-level systemic inflammation. This study was funded by the Spanish Ministry of Science and Innovation MCIN/AEI (RTI2018-098071-B-I00) and it was co-funded by the European Union through the ERDF (Multiregional operative program for Spain 2014–2020). Peer reviewed 2023-03-08T08:40:21Z 2023-03-08T08:40:21Z 2023-02-16 artículo http://purl.org/coar/resource_type/c_6501 Chemico-biological interactions 373: 110404 (2023) 0009-2797 http://hdl.handle.net/10261/296901 10.1016/j.cbi.2023.110404 http://dx.doi.org/10.13039/501100000780 http://dx.doi.org/10.13039/501100011033 36791901 2-s2.0-85148963688 https://api.elsevier.com/content/abstract/scopus_id/85148963688 en #PLACEHOLDER_PARENT_METADATA_VALUE# info:eu-repo/grantAgreement/AEI/Plan Estatal de Investigación Científica y Técnica y de Innovación 2017-2020/RTI2018-098071-B-I00/ES/ESTRATEGIAS PARA MITIGAR LA TOXICIDAD ASOCIADA A LA EXPOSICION CRONICA A ARSENICO O MERCURIO A TRAVES DE LA DIETA/ Chemico-biological interactions Postprint https://doi.org/10.1016/j.cbi.2023.110404 Sí open Elsevier
institution IATA ES
collection DSpace
country España
countrycode ES
component Bibliográfico
access En linea
databasecode dig-iata-es
tag biblioteca
region Europa del Sur
libraryname Biblioteca del IATA España
language English
topic Barrier impairment
Inflammation
Inorganic arsenic
Intestinal microbiota
Intestinal mucosa
Metabolic endotoxemia
http://metadata.un.org/sdg/3
Ensure healthy lives and promote well-being for all at all ages
Barrier impairment
Inflammation
Inorganic arsenic
Intestinal microbiota
Intestinal mucosa
Metabolic endotoxemia
http://metadata.un.org/sdg/3
Ensure healthy lives and promote well-being for all at all ages
spellingShingle Barrier impairment
Inflammation
Inorganic arsenic
Intestinal microbiota
Intestinal mucosa
Metabolic endotoxemia
http://metadata.un.org/sdg/3
Ensure healthy lives and promote well-being for all at all ages
Barrier impairment
Inflammation
Inorganic arsenic
Intestinal microbiota
Intestinal mucosa
Metabolic endotoxemia
http://metadata.un.org/sdg/3
Ensure healthy lives and promote well-being for all at all ages
Domene, Adrián
Orozco, Helena
Rodríguez Viso, Pilar
Monedero, Vicente
Zúñiga, Manuel
Vélez, Dinoraz
Devesa, Vicenta
Intestinal homeostasis disruption in mice chronically exposed to arsenite-contaminated drinking water
description Chronic exposure to inorganic arsenic [As(III) and As(V)] affects about 200 million people, and is linked to a greater incidence of certain types of cancer. Drinking water is the main route of exposure, so, in endemic areas, the intestinal mucosa is constantly exposed to the metalloid. However, studies on the intestinal toxicity of inorganic As are scarce. The objective of this study was to evaluate the toxicity of a chronic exposure to As(III) on the intestinal mucosa and its associated microbiota. For this purpose, BALB/c mice were exposed during 6 months through drinking water to As(III) (15 and 30 mg/L). Treatment with As(III) increased reactive oxygen species (43-64%) and lipid peroxidation (8-51%). A pro-inflammatory response was also observed, evidenced by an increase in fecal lactoferrin (23-29%) and mucosal neutrophil infiltration. As(III) also induced an increase in the colonic levels of pro-inflammatory cytokines (24-201%) and the activation of some pro-inflammatory signaling pathways. Reductions in the number of goblet cells and mucus production were also observed. Moreover, As(III) exposure resulted in changes in gut microbial alpha diversity but no differences in beta diversity. This suggested that the abundance of some taxa was significantly affected by As(III), although the composition of the population did not show significant alterations. Analysis of differential taxa agreed with this, 21 ASVs were affected in abundance or variability, especially ASVs from the family Muribaculaceae. Intestinal microbiota metabolism was also affected, as reductions in fecal concentration of short-chain fatty acids were observed. The effects observed on different components of the intestinal barrier may be responsible of the increased permeability in As(III) treated mice, evidenced by an increase in fecal albumin (48-66%). Moreover, serum levels of Lipopolysaccharide binding proteins and TNF-α were increased in animals treated with 30 mg/L of As(III), suggesting a low-level systemic inflammation.
author2 Agencia Estatal de Investigación (España)
author_facet Agencia Estatal de Investigación (España)
Domene, Adrián
Orozco, Helena
Rodríguez Viso, Pilar
Monedero, Vicente
Zúñiga, Manuel
Vélez, Dinoraz
Devesa, Vicenta
format artículo
topic_facet Barrier impairment
Inflammation
Inorganic arsenic
Intestinal microbiota
Intestinal mucosa
Metabolic endotoxemia
http://metadata.un.org/sdg/3
Ensure healthy lives and promote well-being for all at all ages
author Domene, Adrián
Orozco, Helena
Rodríguez Viso, Pilar
Monedero, Vicente
Zúñiga, Manuel
Vélez, Dinoraz
Devesa, Vicenta
author_sort Domene, Adrián
title Intestinal homeostasis disruption in mice chronically exposed to arsenite-contaminated drinking water
title_short Intestinal homeostasis disruption in mice chronically exposed to arsenite-contaminated drinking water
title_full Intestinal homeostasis disruption in mice chronically exposed to arsenite-contaminated drinking water
title_fullStr Intestinal homeostasis disruption in mice chronically exposed to arsenite-contaminated drinking water
title_full_unstemmed Intestinal homeostasis disruption in mice chronically exposed to arsenite-contaminated drinking water
title_sort intestinal homeostasis disruption in mice chronically exposed to arsenite-contaminated drinking water
publisher Elsevier
publishDate 2023-02-16
url http://hdl.handle.net/10261/296901
http://dx.doi.org/10.13039/501100000780
http://dx.doi.org/10.13039/501100011033
https://api.elsevier.com/content/abstract/scopus_id/85148963688
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